A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017619



Internal ID19106836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20055624..20119044hg38UCSC Ensembl
Innerchr5:20055733..20119153hg19UCSC Ensembl
Innerchr5:20091490..20154910hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3863421
hg1963421
hg1863421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635918
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017619
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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